Pilot Study to Measure Uric Acid in Traumatized Patients: Determinants and Prognostic Association
NCT ID: NCT03622632
Last Updated: 2020-02-18
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
25 participants
OBSERVATIONAL
2018-09-30
2020-09-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
* ≤ 3h after trauma
* ISS ≥ 16
* Received at least 1L of fluid at ER entrance
Exclusion Criteria
* Isolated spine injury
* Chemotherapy within the last month
* Hematologic disease
* Chronic hemodialysis
* Uricase treatment within the last week
* Expected death within 48h
18 Years
ALL
No
Sponsors
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Fonds de la Recherche en Santé du Québec
OTHER_GOV
Centre Integre Universitaire de Sante et Services Sociaux du Nord de l'ile de Montreal
OTHER
Responsible Party
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Emmanuel Charbonney
MD PhD
Locations
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Hôpital du Sacré-Cœur de Montréal
Montreal, Quebec, Canada
Countries
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Other Identifiers
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263425
Identifier Type: -
Identifier Source: org_study_id
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